DE3886766D1 - METHOD FOR PRODUCING TWO-TEED LIGANDS. - Google Patents
METHOD FOR PRODUCING TWO-TEED LIGANDS.Info
- Publication number
- DE3886766D1 DE3886766D1 DE88910206T DE3886766T DE3886766D1 DE 3886766 D1 DE3886766 D1 DE 3886766D1 DE 88910206 T DE88910206 T DE 88910206T DE 3886766 T DE3886766 T DE 3886766T DE 3886766 D1 DE3886766 D1 DE 3886766D1
- Authority
- DE
- Germany
- Prior art keywords
- independently selected
- cycloaliphatic
- aryl
- alkyl
- carbons
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000003446 ligand Substances 0.000 title abstract 3
- 238000004519 manufacturing process Methods 0.000 title 1
- 125000003118 aryl group Chemical group 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000002877 alkyl aryl group Chemical group 0.000 abstract 2
- 125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- -1 e.g. Chemical group 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 125000001624 naphthyl group Chemical group 0.000 abstract 2
- 125000005561 phenanthryl group Chemical group 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 239000000376 reactant Substances 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 125000004423 acyloxy group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 125000001589 carboacyl group Chemical group 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 239000003638 chemical reducing agent Substances 0.000 abstract 1
- 230000008878 coupling Effects 0.000 abstract 1
- 238000010168 coupling process Methods 0.000 abstract 1
- 238000005859 coupling reaction Methods 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 150000002816 nickel compounds Chemical class 0.000 abstract 1
- 239000003880 polar aprotic solvent Substances 0.000 abstract 1
- 238000006479 redox reaction Methods 0.000 abstract 1
- 150000003460 sulfonic acids Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/50—Organo-phosphines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/50—Organo-phosphines
- C07F9/5027—Polyphosphines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/50—Organo-phosphines
- C07F9/505—Preparation; Separation; Purification; Stabilisation
- C07F9/5063—Preparation; Separation; Purification; Stabilisation from compounds having the structure P-H or P-Heteroatom, in which one or more of such bonds are converted into P-C bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Crystallography & Structural Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
A process is disclosed for preparing bidentate ligands of the formula: <IMAGE> wherein: each Ar is independently selected from aromatic ring compounds having 6 up to 14 carbon atoms, e.g., phenyl, naphthyl, phenanthryl and anthracenyl; the x bonds and the y bonds are attached to adjacent carbon atoms on the ring structures; each R, when present as a substituent, is independently selected from alkyl, alkoxy, aryloxy, aryl, aralyky, alkaryl, alkoxyalky, cycloaliphatic, halogen, alkanoyl, alkanoyloxy, alkoxycarbonyl, carboxyl, cyano or formyl radicals; n is a whole number in the range of 0-4 where Ar is phenyl; 0-6 where Ar is naphthyl; and 0-8 where Ar is phenanthryl or anthracenyl; each R1 and R2 is independently selected from alkyl, aryl, aralkyl, alkaryl or cycloaliphatic radicals, or substituted derivatieves thereof; each R3 and R4 is independently selected from hydrogen and the R1 substituents; each of the above alkyl groups or moieties is straight or branched chain of 1-20 carbons; each aryl group contains 6-10 ring carbons; each cycloaliphatic group contains from 4-8 ring carbons; substituted derivatives include others, amines, amides, sulfonic acids, esters, hydroxyl groups and alkoxy groups. The invention process comprises coupling two molecules of a reactant of the formula: <IMAGE> wherein X is halogen, by maintaining a redox reaction system comprising said reactant, a polar aprotic solvent, a nickel compound and a reducing agent at a temperature and for a time sufficient to form the desired bidentate ligand.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/118,573 US4879008A (en) | 1987-11-09 | 1987-11-09 | Preparation of bidentate ligands |
| PCT/US1988/003852 WO1989004315A2 (en) | 1987-11-09 | 1988-10-31 | A process for the preparation of bidentate ligands |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE3886766D1 true DE3886766D1 (en) | 1994-02-10 |
| DE3886766T2 DE3886766T2 (en) | 1994-07-28 |
Family
ID=22379435
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE3886766T Expired - Lifetime DE3886766T2 (en) | 1987-11-09 | 1988-10-31 | METHOD FOR PRODUCING TWO-TEED LIGANDS. |
Country Status (8)
| Country | Link |
|---|---|
| US (3) | US4879008A (en) |
| EP (1) | EP0386105B1 (en) |
| JP (1) | JP2801237B2 (en) |
| KR (2) | KR960002272B1 (en) |
| AT (1) | ATE99314T1 (en) |
| CA (1) | CA1326241C (en) |
| DE (1) | DE3886766T2 (en) |
| WO (1) | WO1989004315A2 (en) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2005504C (en) * | 1988-12-22 | 1995-10-24 | Eastman Chemical Company | Preparation of bidentate ligands |
| JPH0733392B2 (en) * | 1989-06-16 | 1995-04-12 | 高砂香料工業株式会社 | 2,2'-bis [di (m-tolyl) phosphino] -1,1'-binaphthyl |
| DE4020184A1 (en) * | 1990-06-25 | 1992-01-02 | Hoechst Ag | PARTIAL FLUORINE BIPHENYLE, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE |
| JPH0474192A (en) * | 1990-07-12 | 1992-03-09 | Takasago Internatl Corp | 2,2'-bis(dicyclopentylphosphino)-1,1'-binaphthyl and transition metal complex comprising the same compound as ligand |
| DK0579797T3 (en) * | 1992-01-31 | 1999-10-25 | Hoffmann La Roche | diphosphinic |
| DE4433294A1 (en) * | 1993-11-13 | 1995-05-18 | Hoechst Ag | Process for the preparation of bis- (diaryl-alkyl) -phoshines and new compounds from this group of substances |
| US5399771A (en) * | 1994-06-01 | 1995-03-21 | Merck & Co., Inc. | Process of synthesizing binaphthyl derivatives |
| JP3789508B2 (en) * | 1995-03-14 | 2006-06-28 | 高砂香料工業株式会社 | Optically active asymmetric diphosphine and method for obtaining optically active substance in the presence of the compound |
| US6333435B1 (en) | 1995-05-18 | 2001-12-25 | Merck & Co., Inc. | Process of synthesizing binaphthyl derivatives |
| WO1997013763A1 (en) * | 1995-10-13 | 1997-04-17 | The Penn State Research Foundation | Asymmetric synthesis catalyzed by transition metal complexes with new chiral ligands |
| JP3441605B2 (en) * | 1996-10-30 | 2003-09-02 | 高砂香料工業株式会社 | Novel optically active diphosphine, transition metal complex obtained from the compound, and method for obtaining optically active substance in the presence of the complex |
| US5874628A (en) * | 1997-03-26 | 1999-02-23 | Monsanto Company | Method for preparation of tertiary phosphines via nickel-catalyzed cross coupling |
| US6162929A (en) * | 1997-12-23 | 2000-12-19 | Hoffmann-La Roche Inc. | Process for the manufacture of bisphosphine oxide and bisphosphonate compounds |
| GB9805348D0 (en) * | 1998-03-16 | 1998-05-06 | Ici Plc | Compound |
| US20020131972A1 (en) * | 1998-05-21 | 2002-09-19 | Daniel Sem | Multi-partite ligands and methods of identifying and using same |
| US7653490B2 (en) | 2001-09-10 | 2010-01-26 | Triad Liquidating Company LLC | Nuclear magnetic resonance assembly of chemical entities |
| US8513468B2 (en) | 2010-12-30 | 2013-08-20 | Eastman Chemical Company | Process for removing degradation acids from hydroformylation reactions |
| CN102875598B (en) * | 2011-07-11 | 2016-09-07 | 深圳市有为化学技术有限公司 | (diphenyl phosphinyl groups) (mesitylene base) ketone and the preparation method of (phosphniline epoxide) double (mesitylene base ketone) |
| CN109928987B (en) * | 2017-12-19 | 2021-12-21 | 北京颖泰嘉和生物科技有限公司 | Method for preparing o-chlorobenzyl magnesium chloride compound |
| CN111138461B (en) * | 2019-12-05 | 2023-01-20 | 海利尔药业集团股份有限公司 | Continuous preparation method of o-chlorobenzyl chloride Grignard reagent |
| CN113912646B (en) * | 2021-11-18 | 2024-05-17 | 浙江新化化工股份有限公司 | Preparation method of bidentate phosphine ligand |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3239566A (en) * | 1960-07-22 | 1966-03-08 | Shell Oil Co | Hydroformylation of olefins |
| US3539622A (en) * | 1966-12-23 | 1970-11-10 | Hercules Inc | Process for producing diaryl compounds |
| US3527809A (en) * | 1967-08-03 | 1970-09-08 | Union Carbide Corp | Hydroformylation process |
| US3748350A (en) * | 1969-12-29 | 1973-07-24 | Hercules Inc | Coupling with a palladium salt |
| US3636168A (en) * | 1969-12-29 | 1972-01-18 | Hercules Inc | Preparation of polynuclear aromatic compounds |
| US4138420A (en) * | 1976-01-19 | 1979-02-06 | Celanese Corporation | Hydroformylation catalysts |
| US4193943A (en) * | 1976-01-19 | 1980-03-18 | Celanese Corporation | Hydroformylation catalysts |
| US4026957A (en) * | 1976-04-30 | 1977-05-31 | Iowa State University Research Foundation, Inc. | Symmetrical conjugated diene and polyene synthesis via vinylmercuric salts |
| US4139565A (en) * | 1977-03-31 | 1979-02-13 | Celanese Corporation | Hydroformylation using improved catalysts comprising rhodium and diphosphino ligands |
| US4152344A (en) * | 1977-08-08 | 1979-05-01 | Celanese Corporation | Phosphino-ferrocene ligands |
| US4201728A (en) * | 1977-08-19 | 1980-05-06 | Celanese Corporation | Hydroformylation catalyst and process |
| US4169861A (en) * | 1977-08-19 | 1979-10-02 | Celanese Corporation | Hydroformylation process |
| JPS5439059A (en) * | 1977-08-26 | 1979-03-24 | Nitto Riken Kogyo Kk | Production and use of novel phosphine compound |
| JPS54119407A (en) * | 1978-03-09 | 1979-09-17 | Agency Of Ind Science & Technol | Preparation of aldehydes |
| US4263466A (en) * | 1978-10-30 | 1981-04-21 | Union Carbide Corporation | Coupling of aryl and heteroaryl mono chlorides |
| US4221744A (en) * | 1978-12-01 | 1980-09-09 | Celanese Corporation | Hydroformylation process employing rhodium-based catalysts comprising ligands having electronegative substituents |
| US4326989A (en) * | 1979-09-11 | 1982-04-27 | Union Carbide Corporation | Catalyst of nickel compound and ligand in presence of a reducing metal |
| US4760194A (en) * | 1987-02-18 | 1988-07-26 | Eastman Kodak Company | Low pressure hydroformylation catalyst employing unique ligands and process using same |
| US4694109A (en) * | 1986-06-13 | 1987-09-15 | Eastman Kodak Company | Chelate ligands for low pressure hydroformylation catalyst and process employing same |
-
1987
- 1987-11-09 US US07/118,573 patent/US4879008A/en not_active Expired - Lifetime
-
1988
- 1988-10-24 CA CA000581076A patent/CA1326241C/en not_active Expired - Fee Related
- 1988-10-31 EP EP88910206A patent/EP0386105B1/en not_active Expired - Lifetime
- 1988-10-31 JP JP63509391A patent/JP2801237B2/en not_active Expired - Lifetime
- 1988-10-31 KR KR1019950704538A patent/KR960002272B1/en not_active IP Right Cessation
- 1988-10-31 AT AT88910206T patent/ATE99314T1/en not_active IP Right Cessation
- 1988-10-31 WO PCT/US1988/003852 patent/WO1989004315A2/en active IP Right Grant
- 1988-10-31 DE DE3886766T patent/DE3886766T2/en not_active Expired - Lifetime
- 1988-10-31 KR KR1019890701274A patent/KR960002274B1/en not_active IP Right Cessation
-
1989
- 1989-07-24 US US07/383,696 patent/US4956055A/en not_active Expired - Lifetime
- 1989-07-24 US US07/383,697 patent/US4954227A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| US4954227A (en) | 1990-09-04 |
| JP2801237B2 (en) | 1998-09-21 |
| WO1989004315A2 (en) | 1989-05-18 |
| US4879008A (en) | 1989-11-07 |
| KR960002274B1 (en) | 1996-02-14 |
| JPH03500881A (en) | 1991-02-28 |
| DE3886766T2 (en) | 1994-07-28 |
| ATE99314T1 (en) | 1994-01-15 |
| KR960002272B1 (en) | 1996-02-14 |
| KR890701602A (en) | 1989-12-21 |
| EP0386105B1 (en) | 1993-12-29 |
| CA1326241C (en) | 1994-01-18 |
| US4956055A (en) | 1990-09-11 |
| EP0386105A1 (en) | 1990-09-12 |
| WO1989004315A3 (en) | 1989-06-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8364 | No opposition during term of opposition | ||
| 8327 | Change in the person/name/address of the patent owner |
Owner name: EASTMAN CHEMICAL CO., KINGSPORT, TENN., US |